| Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas AL Coste, B Romagnolo, P Billuart, CA Renard, MA Buendia, O Soubrane, ... Proceedings of the National Academy of Sciences 95 (15), 8847-8851, 1998 | 1381 | 1998 |
| A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome V Des Portes, JM Pinard, P Billuart, MC Vinet, A Koulakoff, A Carrié, ... Cell 92 (1), 51-61, 1998 | 861 | 1998 |
| Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation P Billuart, T Bienvenu, N Ronce, V Des Portes, MC Vinet, R Zemni, ... Nature 392 (6679), 923-926, 1998 | 604 | 1998 |
| X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes H Hu, SA Haas, J Chelly, H Van Esch, M Raynaud, APM de Brouwer, ... Molecular psychiatry 21 (1), 133-148, 2016 | 305 | 2016 |
| A new gene involved in X-linked mental retardation identified by analysis of an X; 2 balanced translocation R Zemni, T Bienvenu, MC Vinet, A Sefiani, A Carrié, P Billuart, ... Nature genetics 24 (2), 167-170, 2000 | 296 | 2000 |
| Regulating axon branch stability: the role of p190 RhoGAP in repressing a retraction signaling pathway P Billuart, CG Winter, A Maresh, X Zhao, L Luo Cell 107 (2), 195-207, 2001 | 282 | 2001 |
| Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity M Khelfaoui, C Denis, E van Galen, F de Bock, A Schmitt, C Houbron, ... Journal of Neuroscience 27 (35), 9439-9450, 2007 | 152 | 2007 |
| The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain F Fauchereau, U Herbrand, P Chafey, A Eberth, A Koulakoff, MC Vinet, ... Molecular and Cellular Neuroscience 23 (4), 574-586, 2003 | 135 | 2003 |
| A postsynaptic signaling pathway that may account for the cognitive defect due to IL1RAPL1 mutation A Pavlowsky, A Gianfelice, M Pallotto, A Zanchi, H Vara, M Khelfaoui, ... Current Biology 20 (2), 103-115, 2010 | 129 | 2010 |
| A mosaic genetic screen for genes necessary for Drosophilamushroom body neuronal morphogenesis JE Reuter, TM Nardine, A Penton, P Billuart, EK Scott, T Usui, T Uemura, ... Oxford University Press for The Company of Biologists Limited 130 (6), 1203-1213, 2003 | 118 | 2003 |
| Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia G Zanni, Y Saillour, M Nagara, P Billuart, L Castelnau, C Moraine, ... Neurology 65 (9), 1364-1369, 2005 | 114 | 2005 |
| Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation M Khelfaoui, A Pavlowsky, AD Powell, P Valnegri, KW Cheong, Y Blandin, ... Human molecular genetics 18 (14), 2575-2583, 2009 | 101 | 2009 |
| Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor T Bienvenu, V Des Portes, A Saint Martin, N McDonell, P Billuart, A Carrié, ... Human molecular genetics 7 (8), 1311-1315, 1998 | 100 | 1998 |
| IL-38 ameliorates skin inflammation and limits IL-17 production from γδ T cells Y Han, J Mora, A Huard, P da Silva, S Wiechmann, M Putyrski, C Schuster, ... Cell reports 27 (3), 835-846. e5, 2019 | 90 | 2019 |
| Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse DC Ung, G Iacono, H Méziane, E Blanchard, MA Papon, M Selten, ... Molecular psychiatry 23 (5), 1356-1367, 2018 | 81 | 2018 |
| Emerging major synaptic signaling pathways involved in intellectual disability A Pavlowsky, J Chelly, P Billuart Molecular psychiatry 17 (7), 682-693, 2012 | 79 | 2012 |
| Doublecortin interacts with μ subunits of clathrin adaptor complexes in the developing nervous system G Friocourt, P Chafey, P Billuart, A Koulakoff, MC Vinet, BT Schaar, ... Molecular and Cellular Neuroscience 18 (3), 307-319, 2001 | 78 | 2001 |
| Astrocytes close the mouse critical period for visual plasticity J Ribot, R Breton, CF Calvo, J Moulard, P Ezan, J Zapata, K Samama, ... Science 373 (6550), 77-81, 2021 | 76 | 2021 |
| A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbα P Valnegri, M Khelfaoui, O Dorseuil, S Bassani, C Lagneaux, A Gianfelice, ... Nature neuroscience 14 (10), 1293-1301, 2011 | 73 | 2011 |
| Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes C Delépine, H Meziane, J Nectoux, M Opitz, AB Smith, C Ballatore, ... Human molecular genetics 25 (1), 146-157, 2016 | 69 | 2016 |
